RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      검색결과 좁혀 보기

      선택해제

      오늘 본 자료

      • 오늘 본 자료가 없습니다.
      더보기
      • 무료
      • 기관 내 무료
      • 유료
      • Finding a New Type of Drug Candidate Using Combinatorial Library Approaches

        김성건,Alex G. Cole,Connie G. Tang,윤문영 한국바이오칩학회 2007 BioChip Journal Vol.1 No.4

        As the consequence of an ever-increasing trend toward bacterial antibiotic drug resistance, scientists are compelled to constantly develop a great diversity of mole-cules that can function as potent antibiotics. Using combinatorial library methods, a number of potential drugs can be selected from a sizeable pool of antibiotics. The several molecules selected and described herein, which generally inhibit specific enzymatic activities, show promise in medical applications, including inhibitors of metallo- β-lactamase in <i>B. cereus</i> and of acetohydroxyacid synthase in <i>M. tuberculosis</i>. These potential antibiotics evidence different structures than are exhibited by the currently-used inhibitors, thus raising the possibility that an entirely new class of antibiotics has been found. Combinatorial methods may also be utilized to explore inhibitor specificity, as was previously done using both metallo-β-lactamase and acetohydroxyacid synthase. The isolation of these molecules and the exploration of their specificity underlines the importance and potential of combinatorial methods in the discovery of future antibiotics to combat changing bacterial antibiotic resistance.

      연관 검색어 추천

      이 검색어로 많이 본 자료

      활용도 높은 자료

      해외이동버튼